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Ziprasidone and amisulpride effectively treat negative symptoms of schizophrenia: results of a 12-week, double-blind study.

机译:齐普西酮和氨磺必利可有效治疗精神分裂症的阴性症状:一项为期12周的双盲研究的结果。

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We compared the efficacy of ziprasidone and amisulpride in the treatment of negative symptoms and overall psychopathology in subjects who had chronic schizophrenia with predominantly negative symptoms. This multicentre, 12-week, double-blind study randomly assigned subjects with predominantly negative-symptom schizophrenia [i.e. Positive and Negative Syndrome Scale (PANSS) Negative Subscale score >or=6 points greater than Positive Subscale score] to ziprasidone (40-80 mg b.i.d.; n=60) or amisulpride (50-100 mg b.i.d.; n=63). The primary efficacy variable was the change from baseline in PANSS Negative Subscale score. Secondary efficacy variables included change in scores for PANSS Total, Global Assessment of Functioning, Brief Psychiatric Rating Scale derived from PANSS Total and Core, Clinical Global Impression (CGI)-Severity and CGI-Improvement. For the change in PANSS Negative Subscale score, a ratio to assess the equivalence of the treatment groups was calculated from the least squares mean changes from baseline, with equivalence claimed if the lower limit of the 95% confidence interval of the ratio exceeded 0.60. Mean daily dose, adjusted for differential numbers of subjects and differential days between visits, was 118.0 mg for ziprasidone and 144.7 mg for amisulpride. Mean PANSS Negative Subscale scores improved over the 12-week treatment period for intent-to-treat subjects, evaluable subjects (subjects with >or=4 weeks of double-blind treatment and no protocol deviations) and completers in both treatment groups. Ziprasidone demonstrated efficacy comparable to amisulpride in improving negative symptoms and global psychopathology. The groups demonstrated comparable improvements in secondary efficacy variables. Both agents were generally well tolerated, with comparably low incidences of movement disorders. In subjects with negative symptom-prominent schizophrenia, ziprasidone in mean daily doses of 118 mg was equivalent to amisulpride in mean daily doses of 148 mg in ameliorating negative symptoms and comparable in improving overall psychopathology and global illness severity.
机译:我们比较了齐拉西酮和氨磺必利在慢性精神分裂症患者中主要表现为阴性症状的阴性症状和整体心理病理学的疗效。这项多中心,为期12周的双盲研究随机分配了主要为阴性症状的精神分裂症患者。阳性和阴性综合征量表(PANSS)负子量表得分>或=比正子量表得分高6分]至齐拉西酮(40-80 mg b.i.d .; n = 60)或氨磺必利(50-100 mg b.i.d .; n = 63)。主要功效变量是PANSS负子量表得分相对于基线的变化。次要疗效变量包括PANSS总分的得分变化,整体功能评估,从PANSS总分和核心得出的简短精神病学评定量表,临床总体印象(CGI)-严重性和CGI改善。对于PANSS负子量表得分的变化,根据与基线的最小二乘均值变化计算评估治疗组等效性的比率,如果该比率的95%置信区间的下限超过0.60,则等效。调整的平均日剂量(根据受试者的不同数量和就诊之间的差异天进行调整),齐拉西酮为118.0 mg,氨磺必利为144.7 mg。在两个治疗组中,意向治疗受试者,可评估受试者(双盲治疗≥4周且无方案偏差的受试者)和完成者的PANSS阴性平均量表得分在12周治疗期内均有改善。齐普拉西酮在改善阴性症状和整体精神病理学方面显示出与氨磺必利相当的功效。各组在次级疗效变量方面显示出可比的改善。两种药物通常耐受良好,运动障碍的发生率相对较低。在症状明显的精神分裂症患者中,齐拉西酮的平均日剂量为118 mg相当于氨磺必利的平均日剂量为148 mg,可以减轻阴性症状,并且在改善整体心理病理和总体疾病严重程度方面具有可比性。

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